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Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era
Human immunodeficiency virus (HIV) is a causative agent of acquired immune deficiency syndrome (AIDS). Highly active antiretroviral therapy (HAART) can slow down the replication of HIV-1, leading to an improvement in the survival of HIV-1-infected patients. However, drug toxicities and poor drug adm...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691633/ https://www.ncbi.nlm.nih.gov/pubmed/28961190 http://dx.doi.org/10.3390/v9100281 |
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author | Chupradit, Koollawat Moonmuang, Sutpirat Nangola, Sawitree Kitidee, Kuntida Yasamut, Umpa Mougel, Marylène Tayapiwatana, Chatchai |
author_facet | Chupradit, Koollawat Moonmuang, Sutpirat Nangola, Sawitree Kitidee, Kuntida Yasamut, Umpa Mougel, Marylène Tayapiwatana, Chatchai |
author_sort | Chupradit, Koollawat |
collection | PubMed |
description | Human immunodeficiency virus (HIV) is a causative agent of acquired immune deficiency syndrome (AIDS). Highly active antiretroviral therapy (HAART) can slow down the replication of HIV-1, leading to an improvement in the survival of HIV-1-infected patients. However, drug toxicities and poor drug administration has led to the emergence of a drug-resistant strain. HIV-1 immunotherapy has been continuously developed, but antibody therapy and HIV vaccines take time to improve its efficiency and have limitations. HIV-1-specific chimeric antigen receptor (CAR)-based immunotherapy founded on neutralizing antibodies is now being developed. In HIV-1 therapy, anti-HIV chimeric antigen receptors showed promising data in the suppression of HIV-1 replication; however, autologous transfusion is still a problem. This has led to the development of effective peptides and proteins for an alternative HIV-1 treatment. In this paper, we provide a comprehensive review of potent anti-HIV-1 peptides and proteins that reveal promising therapeutic activities. The inhibitory mechanisms of each therapeutic molecule in the different stages of the HIV-1 life cycle will be discussed herein. |
format | Online Article Text |
id | pubmed-5691633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56916332017-11-22 Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era Chupradit, Koollawat Moonmuang, Sutpirat Nangola, Sawitree Kitidee, Kuntida Yasamut, Umpa Mougel, Marylène Tayapiwatana, Chatchai Viruses Review Human immunodeficiency virus (HIV) is a causative agent of acquired immune deficiency syndrome (AIDS). Highly active antiretroviral therapy (HAART) can slow down the replication of HIV-1, leading to an improvement in the survival of HIV-1-infected patients. However, drug toxicities and poor drug administration has led to the emergence of a drug-resistant strain. HIV-1 immunotherapy has been continuously developed, but antibody therapy and HIV vaccines take time to improve its efficiency and have limitations. HIV-1-specific chimeric antigen receptor (CAR)-based immunotherapy founded on neutralizing antibodies is now being developed. In HIV-1 therapy, anti-HIV chimeric antigen receptors showed promising data in the suppression of HIV-1 replication; however, autologous transfusion is still a problem. This has led to the development of effective peptides and proteins for an alternative HIV-1 treatment. In this paper, we provide a comprehensive review of potent anti-HIV-1 peptides and proteins that reveal promising therapeutic activities. The inhibitory mechanisms of each therapeutic molecule in the different stages of the HIV-1 life cycle will be discussed herein. MDPI 2017-09-29 /pmc/articles/PMC5691633/ /pubmed/28961190 http://dx.doi.org/10.3390/v9100281 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Chupradit, Koollawat Moonmuang, Sutpirat Nangola, Sawitree Kitidee, Kuntida Yasamut, Umpa Mougel, Marylène Tayapiwatana, Chatchai Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era |
title | Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era |
title_full | Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era |
title_fullStr | Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era |
title_full_unstemmed | Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era |
title_short | Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era |
title_sort | current peptide and protein candidates challenging hiv therapy beyond the vaccine era |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691633/ https://www.ncbi.nlm.nih.gov/pubmed/28961190 http://dx.doi.org/10.3390/v9100281 |
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